CS152792A3 - Process for preparing pure enantiomers of n-alkyl-l- or d-amino acids withopen chain - Google Patents

Process for preparing pure enantiomers of n-alkyl-l- or d-amino acids withopen chain Download PDF

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Publication number
CS152792A3
CS152792A3 CS921527A CS152792A CS152792A3 CS 152792 A3 CS152792 A3 CS 152792A3 CS 921527 A CS921527 A CS 921527A CS 152792 A CS152792 A CS 152792A CS 152792 A3 CS152792 A3 CS 152792A3
Authority
CS
Czechoslovakia
Prior art keywords
acyl
alkyl
acid
chain
amino acids
Prior art date
Application number
CS921527A
Other languages
Czech (cs)
English (en)
Inventor
Ulrich Dr Groeger
Karlheinz Dr Drauz
Original Assignee
Degussa
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Degussa filed Critical Degussa
Publication of CS152792A3 publication Critical patent/CS152792A3/cs

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C229/06—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton
    • C07C229/10—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings
    • C07C229/12—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings to carbon atoms of acyclic carbon skeletons
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00—Preparation of nitrogen-containing organic compounds
    • C12P13/04—Alpha- or beta- amino acids
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • C12P41/006—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by reactions involving C-N bonds, e.g. nitriles, amides, hydantoins, carbamates, lactames, transamination reactions, or keto group formation from racemic mixtures
    • C12P41/007—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by reactions involving C-N bonds, e.g. nitriles, amides, hydantoins, carbamates, lactames, transamination reactions, or keto group formation from racemic mixtures by reactions involving acyl derivatives of racemic amines
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/822—Microorganisms using bacteria or actinomycetales
    • Y10S435/874—Pseudomonas

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Analytical Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
CS921527A 1991-05-24 1992-05-21 Process for preparing pure enantiomers of n-alkyl-l- or d-amino acids withopen chain CS152792A3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE4116980A DE4116980A1 (de) 1991-05-24 1991-05-24 Verfahren zur herstellung enantiomerenreiner offenkettiger n-alkyl-l oder d-aminosaeuren

Publications (1)

Publication Number Publication Date
CS152792A3 true CS152792A3 (en) 1992-12-16

Family

ID=6432342

Family Applications (1)

Application Number Title Priority Date Filing Date
CS921527A CS152792A3 (en) 1991-05-24 1992-05-21 Process for preparing pure enantiomers of n-alkyl-l- or d-amino acids withopen chain

Country Status (5)

Country Link
US (1) US5348882A (de)
EP (1) EP0514780A2 (de)
JP (1) JPH05184389A (de)
CS (1) CS152792A3 (de)
DE (1) DE4116980A1 (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2245543A1 (en) * 1996-03-13 1997-09-18 Fabienne Henzen Process for producing n-protected d-proline derivatives 8

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5417030B2 (de) * 1972-12-06 1979-06-27
JPS59203494A (ja) * 1983-05-04 1984-11-17 Sawao Murao Ｎα−カルボベンゾキシアミノ酸アミドヒドロラ−ゼおよびその製法
JPH0783712B2 (ja) * 1987-09-18 1995-09-13 ダイセル化学工業株式会社 新規なプロリンアシラーゼ及びその製造法
DE3929570A1 (de) * 1989-09-06 1991-03-07 Degussa Mikrobiologisch hergestellte n-acyl-l-prolin-acylase, verfahren zu ihrer gewinnung und ihre verwendung
US5219741A (en) * 1989-09-06 1993-06-15 Degussa Ag Method of making L-proline using an N-acyl-L-protine acylase

Also Published As

Publication number Publication date
DE4116980A1 (de) 1992-11-26
EP0514780A2 (de) 1992-11-25
JPH05184389A (ja) 1993-07-27
US5348882A (en) 1994-09-20
EP0514780A3 (de) 1994-04-20

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